Variant #0000334577 (NC_000023.10:g.70389622T>C, NLGN3(NM_018977.3):c.2162T>C)

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.70389622T>C
DNA change (hg38) g.71169772T>C
Published as NLGN3(NM_001166660.1):c.2102T>C (p.(Leu701Pro))
ISCN -
DB-ID NLGN3_000018
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NLGN3 NM_018977.3 ?/. - c.2162T>C r.(?) p.(Leu721Pro)